HRID444316

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3301

Ethylenediamine

C2H8N2

HCID14798

Sodium Hydroxide

HNaO

结构：CC1(C)CC(Nc2nc(Cl)nc(NC3CC(C)(C)NC(C)(C)C3)n2)CC(C)(C)N1

HCID21468017

6-Chloro-N2,N4-bis(2,2,6,6-tetramethyl-4-piperidinyl)-1,3,5-triazine-2,4-diamine

C21H38ClN7

PRODUCTS

生成物

结构：CC1(C)CC(Nc2nc(NCCNc3nc(NC4CC(C)(C)NC(C)(C)C4)nc(NC4CC(C)(C)NC(C)(C)C4)n3)nc(NC3CC(C)(C)NC(C)(C)C3)n2)CC(C)(C)N1

HCID23464889

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID7237

o-Xylene

C8H10

PROCEDURE

实验过程

42.3 (0.1 mole) of 2-chloro-4,6-bis(2,2,6,6-tetramethyl-4-piperidylamino)-1,3,5-triazine (prepared according to example 2A), 3 g (0.05 moles) of ethylenediamine, 4 g of sodium hydroxide and 150 ml of xylene were boiled for 16 hours under stirring.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2b067e7060024897ab2b12d59c2242ee
来源数据集: uspto-grants-1981_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04263434
来源说明: uspto-grants-1981_04

反应 SMILES

Cl[C:2]1[N:7]=[C:6]([NH:8][CH:9]2[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]2)[N:5]=[C:4]([NH:19][CH:20]2[CH2:25][C:24]([CH3:27])([CH3:26])[NH:23][C:22]([CH3:29])([CH3:28])[CH2:21]2)[N:3]=1.[CH2:30]([NH2:33])[CH2:31][NH2:32].[OH-].[Na+]>C1(C)C(C)=CC=CC=1>[CH3:26][C:24]1([CH3:27])[CH2:25][CH:20]([NH:19][C:4]2[N:5]=[C:6]([NH:8][CH:9]3[CH2:14][C:13]([CH3:16])([CH3:15])[NH:12][C:11]([CH3:18])([CH3:17])[CH2:10]3)[N:7]=[C:2]([NH:32][CH2:31][CH2:30][NH:33][C:2]3[N:3]=[C:4]([NH:19][CH:20]4[CH2:25][C:24]([CH3:27])([CH3:26])[NH:23][C:22]([CH3:29])([CH3:28])[CH2:21]4)[N:5]=[C:6]([NH:8][CH:9]4[CH2:10][C:11]([CH3:18])([CH3:17])[NH:12][C:13]([CH3:16])([CH3:15])[CH2:14]4)[N:7]=3)[N:3]=2)[CH2:21][C:22]([CH3:29])([CH3:28])[NH:23]1